K. A. Frolov, B. S. Krivokolysko, N. A. Aksenov, S. G. Krivokolysko
{"title":"(2E,4E)-2-(4-芳基-1,3-硒唑-2-基)-5-苯五-2,4-二烯腈的合成","authors":"K. A. Frolov, B. S. Krivokolysko, N. A. Aksenov, S. G. Krivokolysko","doi":"10.1134/S1070428025600366","DOIUrl":null,"url":null,"abstract":"<p>(2<i>E</i>,4<i>E</i>)-2-Cyano-5-phenylpenta-2,4-dieneselenoamide reacted with α-bromo ketones in DMF under argon to give (2<i>E</i>,4<i>E</i>)-2-(4-aryl-1,3-selenazol-2-yl)-5-phenylpenta-2,4-dienenitriles in 42–71% yields.</p>","PeriodicalId":766,"journal":{"name":"Russian Journal of Organic Chemistry","volume":"61 4","pages":"621 - 624"},"PeriodicalIF":0.9000,"publicationDate":"2025-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of (2E,4E)-2-(4-Aryl-1,3-selenazol-2-yl)-5-phenylpenta-2,4-dienenitriles\",\"authors\":\"K. A. Frolov, B. S. Krivokolysko, N. A. Aksenov, S. G. Krivokolysko\",\"doi\":\"10.1134/S1070428025600366\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>(2<i>E</i>,4<i>E</i>)-2-Cyano-5-phenylpenta-2,4-dieneselenoamide reacted with α-bromo ketones in DMF under argon to give (2<i>E</i>,4<i>E</i>)-2-(4-aryl-1,3-selenazol-2-yl)-5-phenylpenta-2,4-dienenitriles in 42–71% yields.</p>\",\"PeriodicalId\":766,\"journal\":{\"name\":\"Russian Journal of Organic Chemistry\",\"volume\":\"61 4\",\"pages\":\"621 - 624\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-06-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1070428025600366\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1070428025600366","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Synthesis of (2E,4E)-2-(4-Aryl-1,3-selenazol-2-yl)-5-phenylpenta-2,4-dienenitriles
(2E,4E)-2-Cyano-5-phenylpenta-2,4-dieneselenoamide reacted with α-bromo ketones in DMF under argon to give (2E,4E)-2-(4-aryl-1,3-selenazol-2-yl)-5-phenylpenta-2,4-dienenitriles in 42–71% yields.
期刊介绍:
Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.